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1253778-79-8

N-(2-ethoxy-4-methylphenyl)pivalamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1253778-79-8 Structure

  • Basic information

    1. Product Name: N-(2-ethoxy-4-methylphenyl)pivalamide
    2. Synonyms: N-(2-ethoxy-4-methylphenyl)pivalamide
    3. CAS NO:1253778-79-8
    4. Molecular Formula:
    5. Molecular Weight: 235.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1253778-79-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-ethoxy-4-methylphenyl)pivalamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-ethoxy-4-methylphenyl)pivalamide(1253778-79-8)
    11. EPA Substance Registry System: N-(2-ethoxy-4-methylphenyl)pivalamide(1253778-79-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1253778-79-8(Hazardous Substances Data)

1253778-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1253778-79-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,3,7,7 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1253778-79:
(9*1)+(8*2)+(7*5)+(6*3)+(5*7)+(4*7)+(3*8)+(2*7)+(1*9)=188
188 % 10 = 8
So 1253778-79-8 is a valid CAS Registry Number.

1253778-79-8Relevant articles and documents

Remote amide-directed palladium-catalyzed benzylic C-H amination with N-fluorobenzenesulfonimide

Xiong, Tao,Li, Yan,Lv, Yunhe,Zhang, Qian

supporting information; experimental part, p. 6831 - 6833 (2010/10/21)

An unprecedented remote amide-directed palladium-catalyzed intermolecular highly selective benzylic C-H amination with N-fluorobenzenesulfonimide is developed, which represents the first direct benzylic C-H amination with a non-nitrene nitrogen source. This methodology provides a novel approach to circumvent the common ortho aromatic C-H selectivity in directed palladium catalyzed C-H functionalization.

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